|
|
|
|
Manufacturing Supervisor Job
|
| Employer Name: ManufacturingCrossing |
SpiderID: 2256354 |
| Location: Humacao, California |
Date Posted: 6/5/2008 |
| Wage: |
Category: Manufacturing |
| Job Code: 5110585 |
|
Job Description:
RESPONSIBILITIES: 1. Perform operation analysis to maximize flow in the areas and to achieve total product cycle time goals. 2. Assure the best use of resources to obtain a high level of productivity. Establish metrics to monitor employee and area efficiency, utilization and equipment downtime. 3. Identify quality issues related to operator\'s mistakes and establish systems to improve yield, reduce scrap and minimize rework. Establish metrics to monitor employee and area performance in terms of quality. 4. Responsible for the daily WIP analysis and management of daily rates. 5. Perform material analysis to avoid manufacturing disruption, scrap or shortages. 6. Provide the manufacturing direction to coordinators and employees to ensure completion of a daily manufacturing plan as specified by our planning groups. 7. Prepare daily reports on manufacturing achievement, yields and WIP. 8. Responsible of maintain a functional cross training matrix between the employees. 9. Lead improvement projects to optimize the manufacturing processes, including layout changes. 10. Responsible of the correct scrap transaction on a daily basis. 11. Responsible of maintain an accurate inventory (RAW materials and WIP). 12. Lead the weekly cycle counts at manufacturing area. 13. Participate in new product process validation and new product phase review reports. 14. Participate in new product layout and any improvement in process flow. 15. Verify with finance/planning dept status of open work orders in the manufacturing for closure of the orders. 16. Support the preparation of salary plan and department budget. 17. Responsible for maintaining a work environment free of any harassment, discrimination, and high on ethical/quality standards. Promote a safe work environment as established by Medtronic policies & procedures. 18. Perform metrics analysis, Pareto and FMEA as part of line quality issues within validating parameters. 19. Focus on non-value activities elimination. 20. GMP and ISO conformance to the standards. Basic Qualifications EDUCATION: BBA, BS or BSIE. At least 3 years supervisory experience, preferably on a high volume medical device technology company. Knowledge of managing indirectly groups; influencing decisions and enjoys a high level of leadership talent. Good verbal and writing communications skills in English and Spanish Excellent Communication/Presentation Skills Excellent Interpersonal Skills Leads by example and inspires others PC Literate (PC applications such as: Word, Excel, and PowerPoint) Knowledge in JDE systems.
For more information, please click here To visit us at ManufacturingCrossing.
For further information, please visit us online at http://www.manufacturingcrossing.com
Sign Up Now
Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:
Contact Information:
| Contact Name: - |
Company Type: Employer |
| Company: ManufacturingCrossing |
|
|
|
| City: Pasadena |
|
| State: California |
|
| Zip: 91101 |
|
Web Site: http://www.manufacturingcrossing.com
|
|
|
|
|
|
|